Titlebook: Current Directions in Insulin-Like Growth Factor Research; Derek Roith,Mohan K. Raizada Book 1993 The Editor(s) (if applicable) and The Au

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Crayon

Differential Regulation of IGF-I Leader Exon Transcription,cts of these stimuli, its circulating concentrations being sensitive to both GH (Zapf et al., 1981) and nutritional (Prewitt et al., 1982) status. Therefore, in addition to the ubiquitous autocrine/paracrine synthesis of IGF-I by tissues (D’Ercole et al., 1984), circulating IGF-I may exert an import

BRUNT

FLIT

Analysis of the Interaction of IGF-I Analogs with the IGF-I Receptor and IGF Binding Proteins,uble proteins with high affinity for both IGF-I and IGF-II. The type 1 IGF receptor and the IGFBPs appear to form a complex regulatory system for transducing and modulating the activity of IGF-I and IGF-II. The determination of the roles of these proteins in IGF action has been facilitated by the us

Mendicant

交響樂(lè)

交響樂(lè)

Significant Species Differences in Local IGF-I and -II Gene Expression, rodents reflect IGF system function or regulation in other species. For example, IGF-II is usually regarded primarily as a fetal growth factor because its postnatal expression is highly restricted in the rodent. However, in the human and other species, IGF-II levels are equal to or greater than IGF

解脫

Transcriptional Regulation of the Insulin Receptor Gene Promoter,n receptor is a tyrosine kinase. The receptor is a heterotetramer composed of 2 alpha-and 2 beta-subunits. The alpha-subunit is located extracellularly where it binds insulin while the beta-subunit spans the membrane and contains the tyrosine kinase domain. The presence of this receptor is probably

FACT

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